@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_head {
  this: np:hasAssertion dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_assertion ;
    np:hasProvenance dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_provenance ;
    np:hasPublicationInfo dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_provenance a np:Provenance .
  dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0155626 a ncit:C7057 .
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dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_provenance {
  dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_assertion dcterms:description "[Few studies were performed on genetics of the renin-angiotensin-aldosterone system and the results are insufficient and contradictory, such as those about the association between the polymorphism G894T in the eNOS gene or the polymorphism C677T in the MTHFR gene and young AMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:15284679 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP575488.RALuVR-2Eqs7_Wcor-s78H3UAP0DNgELr85o8bcrLjRwM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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